SLV-324 Treatment of Metastatic Solid Tumors

Official title

A Phase 1 Dose-Escalation Study of SLV-324 in Subjects With Metastatic Solid Tumors

Overview

This is a Phase 1 dose-escalation study evaluating the safety, pharmacokinetics, pharmacodynamics, immunogenicity, and efficacy of SLV-324 across a range of dose levels when administered to subjects with metastatic solid tumors.

Detailed description

A Bayesian optimal interval (BOIN) design with a target dose-limiting toxicity (DLT) rate for the maximum tolerated dose (MTD) of 27% and an estimated maximum sample size of \~70 subjects will be used to guide the dose escalation and determine the recommended dosing regimen (RDR) of SLV-324.

SLV-324 will be administered intravenously (IV) in repeated cycles. Treatment will continue until progressive disease or discontinuation.

Interventions

• Drug SLV-324 intravenous (IV infusion)
  SLV-324 will be administered as an IV infusion

Primary outcome measures

• MTD or RDR [Time frame: Through the duration of treatment, up to approximately 18 months]

Secondary outcome measures (12)

• SLV-324 Administration as Assessed by Prescribing Records [Time frame: Through the duration of treatment, up to approximately 18 months]
• SLV-324 Safety [Time frame: Up to approximately 18 months.]
• Evaluation of use of supportive care and other concomitant medications [Time frame: Through the duration of treatment, up to approximately 18 months]
• SLV-324 Pharmacokinetics: Maximum Concentration (Cmax) [Time frame: Varying timepoints through the duration of treatment, up to approximately 18 months]
• Immunogenicity [Time frame: Varying timepoints through the duration of treatment, up to approximately 18 months]
• Objective Response Rate (ORR) [Time frame: Through the duration of treatment, up to approximately 18 months]
• Time to Response (TTR) [Time frame: Up to approximately 36 months]
• Duration of Response (DOR) [Time frame: Up to approximately 36 months.]
• Progression-free Survival (PFS) [Time frame: Up to approximately 36 months]
• Time to Treatment Failure (TTF) [Time frame: Up to approximately 36 months]
• Overall Survival (OS) [Time frame: Up to approximately 36 months]
• SLV-324 Pharmacokinetics: Time to Maximum Concentration (Tmax) [Time frame: Varying timepoints through the duration of treatment, up to approximately 18 months]

Eligibility criteria

Inclusion criteria

• Men or women (as appropriate for cancer type) of age ≥18 years.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
• Histologically or cytologically confirmed diagnosis of solid tumor as documented in medical records.
• Presence of metastatic disease that has progressed during or following previous treatment.
• Presence of radiographically measurable disease.
• Prior receipt of commercially available therapies that are indicated for the subject's cancer and have demonstrated survival benefit for that indication.
• Availability of tumor tissue from a fresh tumor biopsy obtained by a core needle, excisional, or incisional biopsy; or punch biopsy (for cutaneous disease); or archival tumor sample from a previous biopsy.
• Availability of computed tomography (CT) or magnetic resonance imaging (MRI) of chest, abdomen, and pelvis, and/or fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT (if appropriate for tumor type) (with PET from base of the skull to mid-thigh, if performed) within 35 days before study drug administration.
• Completion of all previous therapy (including surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, or investigational therapy) for the treatment of cancer ≥1 week before the start of study drug administration.
• Adequate hematological profile.
• Adequate coagulation profile.
• Adequate hepatic profile.
• Adequate renal function.
• Negative viral serology or adequate therapy for human immunodeficiency virus (HIV), hepatitis B (HBV), and hepatitis C (HCV) infection.
• For female subjects of childbearing potential, a negative serum pregnancy test.
• For female subjects of childbearing potential, willingness to use a protocol-recommended method of contraception from the start of the screening period until ≥6 months after the final dose of study therapy.
• For male subjects who can father a child and are having intercourse with females of childbearing potential who are not using adequate contraception, willingness to use a protocol-recommended method of contraception from the start of study therapy until ≥6 months after the final dose of study therapy and to refrain from sperm donation from the start of study therapy until ≥12 months after administration of the final dose of study therapy.
• Willingness and ability of the subject to comply with scheduled visits, the drug administration plan, protocol-specified laboratory tests, other study procedures (including required tumor biopsy/aspirations and/or radiographic studies), and study restrictions.
• Evidence of a personally signed informed consent indicating that the subject is aware of the neoplastic nature of the disease and has been informed of the procedures to be followed, the experimental nature of the therapy, alternatives, potential risks and discomforts, potential benefits, and other pertinent aspects of study participation.

Exclusion criteria

• Malignancy involving the central nervous system unless brain metastases have been previously treated with radiotherapy, have been stable for ≥4 weeks, and do not require corticosteroids.
• Presence of another cancer with disease manifestations or therapy that could adversely affect subject safety or longevity, create the potential for drug-drug interactions, or compromise the interpretation of study results.
• Uncontrolled ongoing systemic bacterial, fungal, or viral infection (including upper respiratory tract infection) at the time of start of study therapy.
• Significant cardiovascular event or comorbidity.
• Significant screening ECG abnormalities.
• Pregnancy or breastfeeding.
• Major surgery within 4 weeks before the start of study therapy.
• Use of a strong inhibitor or inducer of CYP3A4 or CYP1A2.
• Use of a drug known to prolong the QT interval within 7 days prior to the start of study drug administration.
• Concurrent participation in another therapeutic or imaging clinical trial.
• Other conditions likely to interfere with a subject's ability to participate in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Sequential

Masking

Open label

Primary purpose

Treatment

Study locations

United States · 7 centers

• Hoag Memorial Hospital Presbyterian — Newport Beach
• Washington University — St Louis
• University Hospitals Cleveland Medical Center — Cleveland
• Fox Chase Cancer Center — Philadelphia
• MD Anderson Cancer Center — Houston
• Mays Cancer Center; University of Texas Health San Antonio — Houston
• University of Washington / Fred Hutchinson Cancer Center — Seattle

Identifiers

NCT: NCT07108114 · SLV-324-01Tx

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗